The scientist’s investigation covers issues in Genetics, Genome-wide association study, Disease, Alzheimer's disease and Dementia. Rita Guerreiro usually deals with Genetics and limits it to topics linked to Bioinformatics and Exon. The study incorporates disciplines such as Odds ratio, SORL1 and Genetic association in addition to Genome-wide association study.
Her research integrates issues of Immunology and Medical genetics in her study of Disease. Her Alzheimer's disease research is multidisciplinary, incorporating perspectives in Common disease-common variant, TREM2 and Case-control study. Dementia is the subject of her research, which falls under Internal medicine.
Her scientific interests lie mostly in Genetics, Disease, Genome-wide association study, Dementia and Frontotemporal dementia. Her Genetics study which covers Alzheimer's disease that intersects with TREM2. Her study in Disease is interdisciplinary in nature, drawing from both Allele, Bioinformatics and Genetic architecture.
The Genome-wide association study study combines topics in areas such as Common disease-common variant, Genetic variability, Dementia with Lewy bodies, Genotyping and Genetic association. Her Dementia research is multidisciplinary, incorporating elements of Oncology and Cohort. Rita Guerreiro interconnects Progressive supranuclear palsy, Amyotrophic lateral sclerosis, Neuroscience and Gene mutation in the investigation of issues within Frontotemporal dementia.
Disease, Genetics, Frontotemporal dementia, Internal medicine and Genetic association are her primary areas of study. Her Disease study combines topics in areas such as Polygenic risk score, Single-nucleotide polymorphism and Cerebrospinal fluid. She has researched Single-nucleotide polymorphism in several fields, including PSEN1 and PSEN2.
Her research ties Dystonia and Genetics together. Her work carried out in the field of Internal medicine brings together such families of science as Mutation, Oncology and Genotype. Her research in Genetic association intersects with topics in Genome-wide association study, BCKDK and Genetic architecture.
Rita Guerreiro focuses on Frontotemporal dementia, Genetics, Disease, Genetic association and Gene. Her studies in Frontotemporal dementia integrate themes in fields like Right temporal lobe, Pediatrics, Atrophy and Medical genetics. Her research in Genetics is mostly concerned with Missense mutation.
Her Disease research incorporates elements of Exome sequencing and Immune system. Her work deals with themes such as Loss function, Genome-wide association study, Transcriptome, Nonsynonymous substitution and Genotyping, which intersect with Genetic association. The BCKDK and CNTNAP2 research Rita Guerreiro does as part of her general Gene study is frequently linked to other disciplines of science, such as WWOX and ADAM10, therefore creating a link between diverse domains of science.
This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.
A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD
Alan E. Renton;Elisa Majounie;Adrian James Waite;Javier Simón-Sánchez;Javier Simón-Sánchez.
Neuron (2011)
Erratum: Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease (Nature Genetics (2009) 41 (1088-1093))
D Harold;R Abraham;P Hollingworth;R Sims.
Nature Genetics (2013)
Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease.
Denise Harold;Richard Abraham;Paul Hollingworth;Rebecca Sims.
Nature Genetics (2009)
TREM2 Variants in Alzheimer's Disease
Rita Guerreiro;Rita Guerreiro;Aleksandra Wojtas;Jose Bras;Minerva Carrasquillo.
The New England Journal of Medicine (2013)
Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease
Paul Hollingworth;Denise Harold;Rebecca Sims;Amy Gerrish.
Nature Genetics (2011)
Genotype, haplotype and copy-number variation in worldwide human populations
Mattias Jakobsson;Sonja W. Scholz;Sonja W. Scholz;Paul A Scheet;J. Raphael Gibbs;J. Raphael Gibbs.
Nature (2008)
Genetic evidence implicates the immune system and cholesterol metabolism in the aetiology of Alzheimer's disease.
Lesley Jones;Peter A. Holmans;Marian L. Hamshere;Denise Harold.
PLOS ONE (2010)
Glucocerebrosidase mutations in clinical and pathologically proven Parkinson's disease
Juliane Neumann;Jose Bras;Jose Bras;Emma Deas;Sean S. O'Sullivan.
Brain (2009)
Analysis of shared heritability in common disorders of the brain
Verneri Anttila;Verneri Anttila;Brendan Bulik-Sullivan;Brendan Bulik-Sullivan;Hilary K. Finucane;Raymond K. Walters;Raymond K. Walters.
Science (2018)
Rare coding variants in the phospholipase D3 gene confer risk for Alzheimer’s disease
C Cruchaga;CM Karch;SC Jin;BA Benitez.
Nature (2014)
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